✦ LIBER ✦

Synthesis of N-heterocyclic analogues of 2,5-diaryloxazoles

✍ Scribed by B. M. Krasovitskii; K. M. Dyumaev; L. Sh. Afanasiadi; I. N. Tur; A. A. Verezubova; L. M. Ptyagina

Book ID: 112359589
Publisher: Springer US
Year: 1986
Tongue: English
Weight: 83 KB
Volume: 22
Category: Article
ISSN: 0009-3122
DOI: 10.1007/bf00519954

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Selected Methodologies Convenient for th

Selected Methodologies Convenient for the Synthesis of N ,5-Diaryloxazole-2-amine Pharmacophore

✍ Lintnerová, Lucia; Kováčiková, Lucia; Hanquet, Gilles; Boháč, Andrej 📂 Article 📅 2014 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 931 KB

Heterocyclic Analogues of 5,12-Naphthace

Heterocyclic Analogues of 5,12-Naphthacenequinone. Part 1. Synthesis of Heterocyclic Analogues Starting from 2,3-Diaminoquinizarine.

✍ A. E. Shchekotikhin; I. G. Makarov; V. N. Buyanov; M. N. Preobrazhenskaya 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 21 KB 👁 1 views

Synthesis of Diaryloxazoles 1-3

✍ ALDOUS, DUANE L.; RIEBSOMER, J. L.; CASTLE, RAYMOND N. 📂 Article 📅 1960 🏛 American Chemical Society 🌐 English ⚖ 461 KB

Synthesis of 2,5-diaryloxazoles through

Synthesis of 2,5-diaryloxazoles through friedel-crafts reaction of azlactones with aromatic hydrocarbons

✍ P.T. Frangopol; A.T. Balaban; L. Bǎrlǎdeanu; E. Ciorǎnescu 📂 Article 📅 1961 🏛 Elsevier Science 🌐 French ⚖ 596 KB

Heterocyclization in Vilsmeier-Haack for

Heterocyclization in Vilsmeier-Haack formylation of dimethylamino-substituted 2,5-diaryloxazoles and 2,5-diaryl-1,3,4-oxadiazoles

✍ L. D. Patsenker; I. G. Ermolenko; I. A. Fedyunyaeva; N. A. Popova; B. M. Krasovi 📂 Article 📅 2000 🏛 Springer US 🌐 English ⚖ 115 KB

4,5-Diaryloxazole inhibitors of cyclooxy

4,5-Diaryloxazole inhibitors of cyclooxygenase-2 (COX-2)

✍ John J. Talley; Stephen R. Bertenshaw; David L. Brown; Jeffery S. Carter; Mathew 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 96 KB 👁 1 views

A series of methysulfonyl or sulfonamido substituted 4,5-diaryloxazole were prepared and evaluated for their ability to inhibit the inducible form of cyclooxygenase (COX-2) in vitro and in vivo. Several unique substitution patterns were identified that led to potent and selective inhibitors of COX-2